Dergiler / The Journal of Pediatric Research / 2018 / Cilt: 5 - Sayı: 4

Pediatric Bilateral Pheochromocytoma and Experience of Laparoscopic Cortical Sparing Adrenalectomy

Sayfa
218–220
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We report the experience of laparoscopic bilateral cortical sparing adrenalectomy of a pediatric pheochromocytoma.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Pheochromocytomas are neuroendocrine tumors.
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Temel Bulgular & Veri:In this report, we present a 15-year-old girl who had cerebral palsy and pheochromocytoma.
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Sonuç & Katkı:We report the experience of laparoscopic bilateral cortical sparing adrenalectomy of a pediatric pheochromocytoma.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Pheochromocytomas are neuroendocrine tumors. In this report, we present a 15-year-old girl who had cerebral palsy and pheochromocytoma. She also had a diagnosis of hyperinsulinemic hypoglycemia in her history. She underwent bilateral laparoscopic cortical sparing adrenalectomy. We report the experience of laparoscopic bilateral cortical sparing adrenalectomy of a pediatric pheochromocytoma.

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Bu Makaleye Atıf Yap

ALTINCIK, S. A., ÖZEN, S., ÇELİK, A., DÖKÜMCÜ, Z., DARCAN, Ş., ABACI, A., BÖBER, E. (2018). Pediatric Bilateral Pheochromocytoma and Experience of Laparoscopic Cortical Sparing Adrenalectomy. The Journal of Pediatric Research, Cilt: 5 - Sayı: 4, 218–220. https://ajindex.com/articles/362938

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Kaynakça (6)

  1. Ein SH, Pullerits J, Creighton R, Balfe JW. Pediatric pheochroocytoma. A 36-year review. Pediatr Surg Int 1997;12:595-8.
  2. Waguespack SG, Rich T, Grubbs E, et al. A current review of the etiology, diagnosis and treatment of pediatric pheochromocytoma and paraganglioma. J Clin Endocrinol Metab 2010;95:2023-37.
  3. Martins R, Bugalho MJ. Paragangliomas/Pheochromocytomas: Clinically oriented genetic testing. Int J Endocrinol 2014;2014:794187. Havekes B, Romijn JA, Eisenhofer G, Adams K, Pacak K. Update on pediatric pheochromocytoma. Pediatr Nephrol 2009;24:94350. Choat H, Derrevere K, Knight L, Brown W, Mack EH. SDHBassociated Paraganglioma in a pediatric patient and literature review on hereditary pheochromocytoma-paraganglioma syndromes. Case Rep Endocrinol 2014;2014:502734. Mishra A, Mehrotra PK, Agarwal G, Agarwal A, Mishra SK. Pediatric and adolescent pheochromocytoma: Clinical presentation and outcome of surgery. Indian Pediatr 2014;51:299-302.
  4. Neumann HP, Bausch B, McWhinney SR, et al. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J med 2002;346:1459-66.
  5. Puri S, Cano DA, Hebro M. A role for von Hippel-Lindau protein in pancreatic B cell function. Diabetes 2009;58:433-41.
  6. Puri S, Garcia_Nunez A, Hebrok M, Cano DA. Elimination of Von Hippel-Lindau function perturbs pancreas endocrine homeostatis in mice. PLoS ONE 2013;8:72213. Kurabayashi A, Kakinuma Y, Morita T, Inoue K, Sato T, Furihata M. Conditional VHL gene deletion causes hypoglycemic death associated with disproportionately increased glucose uptake by hepatocytes through an upregulated IGF-1 receptor. PLoS ONE 2013;8:69139.